Substituents drive ligand rearrangements, giving dinuclear rather than mononuclear complexes, and tune CoII/III redox potential
Author:
Affiliation:
1. Department of Chemistry and MacDiarmid Institute of Advanced Materials and Nanotechnology
2. University of Otago
3. Dunedin 9054
4. New Zealand
Abstract
Sterically encumbered 6-halo-substituents lead to BF4/MeOH/ligand rearrangement, forming doubly bridged {Co1–[O(Me)–B(F2)–O(R)]2–Co1A} dinuclear complexes (6-Cl, 6-Br) of the modified ligands.
Funder
University of Otago
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/DT/C8DT01502C
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4. Correction: Substituents drive ligand rearrangements, giving dinuclear rather than mononuclear complexes, and tune CoII/III redox potential;Dalton Transactions;2019
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